Taiwan FDA registration 8b6af8a0eb4039187708d8395c1b1a4e
"Intec" hippocampal renal artery stent system
TW: “英泰克”海馬腎動脈支架系統
Registration details
- Analysis ID
- 8b6af8a0eb4039187708d8395c1b1a4e
- Customs Code
- DHA00602105808
Company information
- Manufacturer
- Invatec S.p.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- May 27, 2010
- Expiry Date
- May 27, 2020
- Cancellation Date
- Mar 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Intec" hippocampal renal artery stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8b6af8a0eb4039187708d8395c1b1a4e and manufactured by Invatec S.p.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices